{
  "id": 9992,
  "label": "acrorenal syndrome, autosomal recessive",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008719",
  "properties": {
    "xrefs": [
      "GARD:0015130",
      "MEDGEN:163241",
      "MESH:C535666",
      "OMIM:201310",
      "UMLS:C0796290"
    ],
    "synonyms": [
      "acrorenal syndrome, autosomal recessive",
      "autosomal recessive acrorenal syndrome",
      "Curran syndrome",
      "acrorenal syndrome autosomal recessive",
      "acrorenal syndrome recessive"
    ],
    "definition": "Autosomal recessive form of acrorenal syndrome."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7611,
      "label": "autosomal recessive disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050737",
          "EFO:1000017",
          "ICD9:758.5",
          "MEDGEN:539209",
          "SCTID:85995004",
          "UMLS:C0265388"
        ],
        "synonyms": [
          "autosomal recessive disease or disorder",
          "autosomal recessive hereditary disease",
          "autosomal recessive hereditary disorder",
          "autosomal recessive inherited disease",
          "autosomal recessive inherited disorder",
          "disease or disorder, autosomal recessive",
          "disease, autosomal recessive",
          "recessive hereditary disorder (autosomal)"
        ],
        "definition": "Autosomal recessive form of disease."
      },
      "child_count": 219,
      "reference_id": "MONDO:0006025"
    },
    {
      "id": 8478,
      "label": "acrorenal syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16089
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060347",
          "GARD:0000514",
          "MEDGEN:501193",
          "MESH:C563159",
          "OMIM:102520",
          "Orphanet:971",
          "SCTID:720458005",
          "UMLS:C3495490",
          "icd11.foundation:1948375645"
        ],
        "synonyms": [
          "acrorenal syndrome"
        ],
        "definition": "Acrorenal syndrome comprises a wide spectrum of congenital malformative disorders characterized by the co-occurrence of distal limb anomalies (usually bilateral cleft feet and/or hands) and renal defects (e.g. unilateral or bilateral agenesis), that can be associated with a variety of other anomalies such as those of genitourinary tract (genital anomalies, ureteral hypoplasias, vesicoureteral reflux), abdominal well defects, intestinal atresias, and lung malformations. Familial cases have been reported in which an autosomal recessive inheritance was suspected."
      },
      "child_count": 1,
      "reference_id": "MONDO:0007059"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7611,
      "label": "autosomal recessive disease"
    },
    {
      "id": 8478,
      "label": "acrorenal syndrome"
    }
  ]
}